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MX2020012137A - Mcl-1 inhibitors. - Google Patents

Mcl-1 inhibitors.

Info

Publication number
MX2020012137A
MX2020012137A MX2020012137A MX2020012137A MX2020012137A MX 2020012137 A MX2020012137 A MX 2020012137A MX 2020012137 A MX2020012137 A MX 2020012137A MX 2020012137 A MX2020012137 A MX 2020012137A MX 2020012137 A MX2020012137 A MX 2020012137A
Authority
MX
Mexico
Prior art keywords
mcl
inhibitors
compounds
methods
present disclosure
Prior art date
Application number
MX2020012137A
Other languages
Spanish (es)
Inventor
Michael L Mitchell
Tetsuya Kobayashi
Chandrasekar Venkataramani
Vickie H Tsui
Scott E Lazerwith
Darryl Kato
Hong Yang
Juan A Guerrero
William J Watkins
Devan Naduthambi
Neil H Squires
Lan Jiang
John E Knox
Hang Chu
Anna E Hurtley
Tae H Hwang
Xiaofen Li
David W Lin
Jonathan W Medley
Zachary Newby
Original Assignee
Gilead Sciences Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Gilead Sciences Inc filed Critical Gilead Sciences Inc
Publication of MX2020012137A publication Critical patent/MX2020012137A/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D267/00Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D267/02Seven-membered rings
    • C07D267/08Seven-membered rings having the hetero atoms in positions 1 and 4
    • C07D267/12Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/553Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D267/00Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D267/02Seven-membered rings
    • C07D267/08Seven-membered rings having the hetero atoms in positions 1 and 4
    • C07D267/12Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • C07D267/16Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with two six-membered rings
    • C07D267/20[b, f]-condensed
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C381/00Compounds containing carbon and sulfur and having functional groups not covered by groups C07C301/00 - C07C337/00
    • C07C381/10Compounds containing sulfur atoms doubly-bound to nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/10Spiro-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/08Bridged systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

La presente descripción se refiere en general a compuestos y composiciones farmacéuticas que se pueden utilizar en métodos para tratar el cáncer.The present disclosure relates generally to compounds and pharmaceutical compositions that can be used in methods of treating cancer.

MX2020012137A 2018-05-14 2019-05-13 Mcl-1 inhibitors. MX2020012137A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201862671306P 2018-05-14 2018-05-14
US201862749918P 2018-10-24 2018-10-24
PCT/US2019/032053 WO2019222112A1 (en) 2018-05-14 2019-05-13 Mcl-1 inhibitors

Publications (1)

Publication Number Publication Date
MX2020012137A true MX2020012137A (en) 2021-01-29

Family

ID=66770559

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2020012137A MX2020012137A (en) 2018-05-14 2019-05-13 Mcl-1 inhibitors.

Country Status (29)

Country Link
US (4) US10703733B2 (en)
EP (2) EP3793565B1 (en)
JP (3) JP6899975B2 (en)
KR (4) KR102666717B1 (en)
CN (2) CN117304130A (en)
AU (3) AU2019269391B2 (en)
BR (1) BR112020021648A2 (en)
CA (1) CA3099152C (en)
CL (1) CL2020002919A1 (en)
CO (1) CO2020014009A2 (en)
CR (1) CR20200544A (en)
CY (1) CY1125065T1 (en)
DK (1) DK3793565T3 (en)
ES (1) ES2907923T3 (en)
HR (1) HRP20220215T1 (en)
HU (1) HUE057852T2 (en)
IL (2) IL291430B2 (en)
LT (1) LT3793565T (en)
MX (1) MX2020012137A (en)
PE (1) PE20210004A1 (en)
PH (1) PH12020551881A1 (en)
PL (1) PL3793565T3 (en)
PT (1) PT3793565T (en)
SG (1) SG11202010964VA (en)
SI (1) SI3793565T1 (en)
TW (3) TWI719478B (en)
UA (1) UA125163C2 (en)
WO (1) WO2019222112A1 (en)
ZA (1) ZA202007007B (en)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117304130A (en) 2018-05-14 2023-12-29 吉利德科学公司 MCL-1 inhibitors
CN114096546A (en) 2019-07-09 2022-02-25 詹森药业有限公司 Macrocyclic spirocyclic derivatives useful as MCL-1 inhibitors
ES2973832T3 (en) 2019-10-18 2024-06-24 Forty Seven Inc Combination therapies for the treatment of myelodysplastic syndromes and acute myeloid leukemia
AU2020374947B2 (en) 2019-10-31 2024-11-14 Forty Seven, LLC Anti-CD47 and anti-CD20 based treatment of blood cancer
TWI778443B (en) * 2019-11-12 2022-09-21 美商基利科學股份有限公司 Mcl1 inhibitors
AU2020391106B2 (en) * 2019-11-26 2024-03-21 Gilead Sciences, Inc. Processes and intermediates for preparing MCL1 inhibitors
JP2023509881A (en) 2019-12-24 2023-03-10 カルナバイオサイエンス株式会社 Diacylglycerol kinase modulating compounds
US20230212191A1 (en) * 2020-04-16 2023-07-06 Prelude Therapeutics, Incorporated Spiro-sulfonimidamide derivatives as inhibitors of myeloid cell leukemia-1 (mcl-1) protein
KR20230023008A (en) * 2020-06-10 2023-02-16 얀센 파마슈티카 엔.브이. Macrocyclic 2-amino-3-fluoro-but-3-enamide as an inhibitor of MCL-1
CA3201943A1 (en) * 2020-11-19 2022-05-27 Gilead Sciences, Inc. Processes and intermediates for preparing mcl1 inhibitors
KR20230121806A (en) 2020-12-17 2023-08-21 얀센 파마슈티카 엔.브이. Macrocyclic branched 3-fluoro-but-3-enamide as an inhibitor of MCL-1
TW202302145A (en) 2021-04-14 2023-01-16 美商基利科學股份有限公司 Co-inhibition of cd47/sirpα binding and nedd8-activating enzyme e1 regulatory subunit for the treatment of cancer
US20240239812A1 (en) 2021-04-26 2024-07-18 Janssen Pharmaceutica Nv Macrocyclic 2-allyltetrahydrofurans as inhibitors of mcl-1
US20220389394A1 (en) 2021-05-18 2022-12-08 Gilead Sciences, Inc. METHODS OF USING FLT3L-Fc FUSION PROTEINS
AU2022291381A1 (en) 2021-06-11 2023-11-30 Gilead Sciences, Inc. Combination mcl-1 inhibitors with anti-cancer agents
KR20240019330A (en) 2021-06-11 2024-02-14 길리애드 사이언시즈, 인코포레이티드 Combination of MCL-1 inhibitor and antibody drug conjugate
EP4359411A1 (en) 2021-06-23 2024-05-01 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
WO2022271684A1 (en) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
JP2024520593A (en) 2021-06-23 2024-05-24 ギリアード サイエンシーズ, インコーポレイテッド DIACYLGLYERCOL KINASE MODULATORY COMPOUNDS
CN117396478A (en) 2021-06-23 2024-01-12 吉利德科学公司 Diacylglycerol kinase modulating compounds
CA3237011A1 (en) 2021-11-16 2023-05-25 Soufyan JERHAOUI Macrocyclic 2-amino-but-3-enamides as inhibitors of mcl-1
EP4499146A1 (en) 2022-03-24 2025-02-05 Gilead Sciences, Inc. Combination therapy for treating trop-2 expressing cancers
TW202345901A (en) 2022-04-05 2023-12-01 美商基利科學股份有限公司 Combination therapy for treating colorectal cancer
KR20250004050A (en) * 2022-05-04 2025-01-07 길리애드 사이언시즈, 인코포레이티드 Salts and polymorphs of specific MCL-1 inhibitors
WO2024064668A1 (en) 2022-09-21 2024-03-28 Gilead Sciences, Inc. FOCAL IONIZING RADIATION AND CD47/SIRPα DISRUPTION ANTICANCER COMBINATION THERAPY

Family Cites Families (62)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6319494B1 (en) 1990-12-14 2001-11-20 Cell Genesys, Inc. Chimeric chains for receptor-associated signal transduction pathways
IL104570A0 (en) 1992-03-18 1993-05-13 Yeda Res & Dev Chimeric genes and cells transformed therewith
US7446190B2 (en) 2002-05-28 2008-11-04 Sloan-Kettering Institute For Cancer Research Nucleic acids encoding chimeric T cell receptors
US7405295B2 (en) 2003-06-04 2008-07-29 Cgi Pharmaceuticals, Inc. Certain imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of Bruton's tyrosine kinase by such compounds
SI3153514T1 (en) 2004-05-13 2022-02-28 Icos Corporation Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta
US20090142345A1 (en) 2005-03-15 2009-06-04 Takeda Pharmaceutical Company Limited Prophylactic/therapeutic agent for cancer
EP2418278A3 (en) 2005-05-09 2012-07-04 Ono Pharmaceutical Co., Ltd. Human monoclonal antibodies to programmed death 1(PD-1) and methods for treating cancer using anti-PD-1 antibodies alone or in combination with other immunotherapeutics
EP2982379A1 (en) 2005-07-01 2016-02-10 E. R. Squibb & Sons, L.L.C. Human monoclonal antibodies to programmed death ligand 1 (pd-l1)
WO2008109943A1 (en) 2007-03-12 2008-09-18 Cytopia Research Pty Ltd Phenyl amino pyrimidine compounds and uses thereof
PT2537529T (en) 2007-08-02 2018-12-12 Gilead Biologics Inc Loxl2 inhibitory antibodies and uses thereof
JP5674155B2 (en) 2008-07-21 2015-02-25 アポゲニクス ゲゼルシャフト ミット ベシュレンクテル ハフツングApogenix GmbH TNFSF single-stranded molecule
US8652843B2 (en) 2008-08-12 2014-02-18 Oncomed Pharmaceuticals, Inc. DDR1-binding agents and methods of use thereof
US8450321B2 (en) 2008-12-08 2013-05-28 Gilead Connecticut, Inc. 6-(1H-indazol-6-yl)-N-[4-(morpholin-4-yl)phenyl]imidazo-[1,2-A]pyrazin-8-amine, or a pharmaceutically acceptable salt thereof, as a SYK inhibitor
TWI625121B (en) 2009-07-13 2018-06-01 基利科學股份有限公司 Inhibitor of kinases that regulate apoptosis signaling
RU2015108348A (en) 2010-02-04 2015-07-20 Джилид Байолоджикс, Инк. ANTIBODIES BINDING WITH LYSYLOXIDASE-LIKE ENZYME-2 (LOXL2), AND WAYS OF THEIR APPLICATION
US9089520B2 (en) 2010-05-21 2015-07-28 Baylor College Of Medicine Methods for inducing selective apoptosis
ES2739505T3 (en) 2010-08-27 2020-01-31 Gilead Biologics Inc Antibodies against matrix metalloproteinase 9
PH12013501201A1 (en) 2010-12-09 2013-07-29 Univ Pennsylvania Use of chimeric antigen receptor-modified t cells to treat cancer
TWI567061B (en) 2011-07-01 2017-01-21 吉李德科學股份有限公司 Compound for the treatment of addiction
JP6101205B2 (en) 2011-08-23 2017-03-22 中外製薬株式会社 Novel anti-DDR1 antibody having antitumor activity
GB201115529D0 (en) 2011-09-08 2011-10-26 Imp Innovations Ltd Antibodies, uses and methods
WO2013052699A2 (en) 2011-10-04 2013-04-11 Gilead Calistoga Llc Novel quinoxaline inhibitors of pi3k
UY34573A (en) 2012-01-27 2013-06-28 Gilead Sciences Inc QUINASE INHIBITOR REGULATING THE APOPTOSIS SIGNAL
WO2013116562A1 (en) 2012-02-03 2013-08-08 Gilead Calistoga Llc Compositions and methods of treating a disease with (s)-4 amino-6-((1-(5-chloro-4-oxo-3-phenyl-3,4-dihydroquinazolin-2-yl)ethyl)amino)pyrimidine-5-carbonitrile
TW201427995A (en) 2012-09-24 2014-07-16 Gilead Sciences Inc Anti-DDR1 antibodies
PT2935246T (en) 2012-12-21 2018-10-10 Gilead Calistoga Llc Isoquinolinone or quinazolinone phosphatidylinositol 3-kinase inhibitors
BR112015014585A2 (en) 2012-12-21 2017-07-11 Gilead Calistoga Llc compound, pharmaceutical composition, and method of treating a human
TWI527811B (en) 2013-05-09 2016-04-01 吉李德科學股份有限公司 Benzimidazole derivatives as bromodomain inhibitors
MX347988B (en) 2013-06-14 2017-05-19 Gilead Sciences Inc Phosphatidylinositol 3-kinase inhibitors.
MD4659B1 (en) 2013-07-30 2019-11-30 Gilead Connecticut Inc Polymorph of SYK inhibitors
TWI735853B (en) 2013-12-23 2021-08-11 美商克洛諾斯生技有限公司 Syk inhibitors
US9290505B2 (en) 2013-12-23 2016-03-22 Gilead Sciences, Inc. Substituted imidazo[1,2-a]pyrazines as Syk inhibitors
US10533010B2 (en) * 2014-03-27 2020-01-14 Vanderbilt University Substituted indole Mcl-1 inhibitors
WO2015157399A1 (en) 2014-04-10 2015-10-15 Seattle Children's Hospital (dba Seattle Children's Research Institute) Transgene genetic tags and methods of use
TWI805109B (en) 2014-08-28 2023-06-11 美商奇諾治療有限公司 Antibodies and chimeric antigen receptors specific for cd19
JO3474B1 (en) * 2014-08-29 2020-07-05 Amgen Inc Tetrahydronaphthalene derivatives that inhibit mcl-1 protein
EA201790395A1 (en) 2014-09-26 2017-08-31 Джилид Сайэнс, Инк. AMINOTRIAZIN DERIVATIVES SUITABLE FOR USING AS TANK-BINDING KINASE INHIBITORS
CN107206025A (en) 2014-12-03 2017-09-26 朱诺治疗学股份有限公司 The method and composition treated for adoptive cellular
US20160166613A1 (en) 2014-12-15 2016-06-16 Bellicum Pharmaceuticals, Inc. Methods for controlled elimination of therapeutic cells
KR20180004811A (en) 2015-05-15 2018-01-12 길리애드 사이언시즈, 인코포레이티드 Benzimidazole and imidazopyridine carboximidamide compounds having activity as an inhibitor of indoleamine 2,3-dioxygenase
JP6949728B2 (en) 2015-05-29 2021-10-13 ジュノー セラピューティクス インコーポレイテッド Compositions and Methods for Modulating Inhibitory Interactions in Genetically Engineered Cells
MX2018003353A (en) 2015-09-17 2018-09-17 Novartis Ag THERAPIES WITH CART CELLS WITH IMPROVED EFFECTIVENESS.
WO2017147410A1 (en) 2016-02-25 2017-08-31 Amgen Inc. Compounds that inhibit mcl-1 protein
JP6453507B2 (en) 2017-03-30 2019-01-16 アムジエン・インコーポレーテツド Compound that inhibits MCL-1 protein
MA49908A (en) 2017-08-18 2021-04-28 Amgen Inc MCL-1 PROTEIN INHIBITORS
US11279712B2 (en) 2017-08-29 2022-03-22 Amgen Inc. Macrocyclic compounds that inhibit MCL-1 protein
US11332459B2 (en) 2017-10-19 2022-05-17 Teijin Pharma Limited Benzimidazole derivatives and their uses
MA54985A (en) 2018-03-05 2021-12-29 Amgen Inc ALPHA-HYDROXY PHENYLACETIC ACID PHARMACOPHORES OR ANTAGONISTS OF BIOISOSTERY MCL-1 PROTEIN
PE20211917A1 (en) 2018-05-14 2021-09-28 Reata Pharmaceuticals Inc BIARYLAMIDES WITH MODIFIED SUGAR GROUPS FOR THE TREATMENT OF DISEASES ASSOCIATED WITH THE TRAJECTORY OF HEAT SHOCK PROTEIN
CN117304130A (en) 2018-05-14 2023-12-29 吉利德科学公司 MCL-1 inhibitors
TW201946906A (en) 2018-05-15 2019-12-16 美商阿拜德生物製藥公司 MAGL inhibitors
MA53377A (en) 2018-07-24 2021-06-02 Epizyme Inc PYRIDIN-2-ONE COMPOUNDS USEFUL AS SMARCA2 ANTAGONISTS
CA3118919A1 (en) 2018-11-09 2020-05-14 Prelude Therapeutics, Incorporated Spiro-sulfonamide derivatives as inhibitors of myeloid cell leukemia-1 (mcl-1) protein
WO2020147802A1 (en) 2019-01-18 2020-07-23 Ascentage Pharma (Suzhou) Co., Ltd. Macrocyclic spiroethers as mcl-1 inhibitors
TWI778443B (en) 2019-11-12 2022-09-21 美商基利科學股份有限公司 Mcl1 inhibitors
AU2020391106B2 (en) 2019-11-26 2024-03-21 Gilead Sciences, Inc. Processes and intermediates for preparing MCL1 inhibitors
JP2021161114A (en) 2020-03-31 2021-10-11 アムジエン・インコーポレーテツド Methylation of Mcl-1 compound
TWI827924B (en) 2020-05-06 2024-01-01 美商安進公司 Ring closing synthesis of macrocyclic mcl-1 inhibitor intermediates
JP2023524263A (en) 2020-05-06 2023-06-09 アムジエン・インコーポレーテツド Synthesis of vinyl-protected alcohol intermediates
KR20230023008A (en) 2020-06-10 2023-02-16 얀센 파마슈티카 엔.브이. Macrocyclic 2-amino-3-fluoro-but-3-enamide as an inhibitor of MCL-1
CA3184877A1 (en) 2020-07-08 2022-01-13 Benoit Christian Albert Ghislain De Boeck Macrocyclic ether containing indole derivatives as inhibitors of mcl-1
CA3201943A1 (en) 2020-11-19 2022-05-27 Gilead Sciences, Inc. Processes and intermediates for preparing mcl1 inhibitors

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